Manager, Clinical Process Improvement

Adecco is currently hiring a Manager, Clinical Process Improvement for our Medical Device Manufacturing client in Ottawa West. This is a contract opportunity offering full time hours, Monday – Friday. The salary for this position will be determined based on education and experience.

Our client is a diversified health care innovator with a legacy of pioneering work in medical diagnostics and devices. They are dedicated to advancing innovative with patient diagnostic technology to improve patient care and system efficiency by fundamentally changing the way health care professionals process patients through their system.

Position Overview: Responsible for management, execution and implementation of continuous improvement programs to drive excellence and deliver improvements and efficiencies within the Global Clinical Affairs group in accordance with GCP and company quality and regulatory compliance. The role will work in close collaboration with the other functions within the Clinical group such as Data Management, Statistics, Contracting, Logistics and Writing as well as working closely with other functions within the company (R&D, Quality, Regulatory and PMO).

Responsibilities:

  • Responsible for leading the implementation of internal process optimization and system/process improvement programs including but not limited to: efficiency in clinical documentation, develop procedures to align with regulations, clinical data management.
  • Lead efforts to define efficient processes, capturing best practices in procedures and documents.
  • Develop tools, systems and dashboards to monitor effectiveness and enhance quality and efficiency in all areas of the Clinical group.
  • Continue to evaluate, develop and implement best practices across all functional areas of the group.
  • Establishes project and leads project planning and execution for clinical improvement initiatives.
  • Able to translate toplevel goals to specific project level goals for team members. May generate and champions new project ideas.
  • Ensure compliance with GCP, quality and regulatory compliance and other site specific requirements.
  • Responsibilities:

  • Bachelor’s degree in Engineering, Biological Science or related medical/scientific field
  • Advanced Degree (M.Sc, Ph.D) is an asset.
  • Minimum 6 years relevant work experience; 3 years directly supporting clinical research or similar experience in a medical/scientific area (IVD or Medical Device preferred)
  • 2-3 years experience managing projects and working with clinical professionals within a team, as well as working in a cross functional product development setting.
  • Knowledge of process improvement techniques is preferred (Six Sigma tools an asset)
  • Expertise with GCPs and regulatory compliance for clinical trials (e.g. applicable ISO Standards, FDA)
  • High attention to detail and accuracy.
  • Advanced written and oral communications skills.
  • Able to manage multiple tasks independently.
  • To be considered for the Manager, Clinical Process Improvement  opportunity, please Apply Now!

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    Reference number CA_EN_1_021956_1711554

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